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Software Process Improvement Roadmapping – A Roadmap for Implementing IEC 62304 in Organizations Developing and Maintaining Medical Device Software

机译:软件过程改进和路线图–在开发和维护医疗设备软件的组织中实施IEC 62304的路线图

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摘要

Organizations engaged in medical device software are required to demonstrate compliance with a set of medical device standards and regulations before the device can be marketed. One such standard IEC 62304, Medical device software -- Software life cycle processes, is a standard that defines the processes that are required to be executed in order to develop safe software. Demonstrating compliance with IEC 62304 can be problematic for organizations that are new to or have limited experience in the domain. The standard defines what processes must be carried out, but does not state how. This paper presents a research method for generating a roadmap that will guide organizations in the implementation of IEC 62304.
机译:从事医疗器械软件开发的组织必须证明其符合一系列医疗器械标准和法规,然后才能销售该设备。一种这样的标准IEC 62304,即“医疗设备软件-软件生命周期过程”是一种标准,它定义了开发安全软件所需执行的过程。对于刚接触该领域或经验有限的组织,证明符合IEC 62304可能会成问题。该标准定义了必须执行哪些过程,但未说明如何执行。本文提出了一种研究路线图的研究方法,该路线图将指导组织实施IEC 62304。

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